Coburn C T, Hajri T, Ibrahimi A, Abumrad N A
Department of Physiology, State University of New York at Stony Brook, 11794-8661, USA.
J Mol Neurosci. 2001 Apr-Jun;16(2-3):117-21; discussion 151-7. doi: 10.1385/JMN:16:2-3:117.
The transmembrane glycoprotein CD36 has been identified in isolated cell studies as a putative transporter of long-chain fatty acids. To examine the physiological role of CD36, we studied FA uptake and metabolism by tissues of CD36 null mice after injection with two fatty acid analogs. Compared to controls, uptake was substantially reduced (50-80%) in heart, skeletal muscle, and adipose tissues of null mice. The reduction in uptake was associated with a large decrease in fatty acid incorporation into triglycerides, which could be accounted for by an accumulation of diacylglycerides. Thus CD36 facilitates a major fraction of fatty acid uptake by myocardial, skeletal muscle, and adipose tissues, where it is highly expressed. Its role in other tissues where its expression is low and cell-specific could not be determined in these studies.
跨膜糖蛋白CD36在分离细胞研究中被鉴定为长链脂肪酸的假定转运体。为了研究CD36的生理作用,我们在给CD36基因敲除小鼠注射两种脂肪酸类似物后,研究了其组织对脂肪酸的摄取和代谢情况。与对照组相比,基因敲除小鼠心脏、骨骼肌和脂肪组织中的摄取量大幅降低(50 - 80%)。摄取量的减少与脂肪酸掺入甘油三酯的大幅下降有关,这可以通过二酰甘油的积累来解释。因此,CD36促进了心肌、骨骼肌和脂肪组织中大部分脂肪酸的摄取,这些组织中CD36高度表达。在这些研究中无法确定其在其他表达量低且具有细胞特异性的组织中的作用。